The trial aims to evaluate whether the Airvo 3 device in OptiO2 mode can maintain patients' SpO2 levels within the target range better than manual oxygen titration in hospitalized COPD patients with hypoxemia/respiratory distress.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
70
Nasal high flow with closed loop oxygen control
Nasal high flow with manual titration
Icahn School of Medicine at Mount Sinai
New York, New York, United States
RECRUITINGPercentage of time with SpO2 in target range over period of observation
Time frame: 24 hours
Percentage of time with SpO2 out of target range over period of observation
Time frame: 24 hours
Count of number of adjustments in FiO2 by clinical staff over observation period
Time frame: 24 hours
Percentage of time with SpO2 above target range over period of observation
Time frame: 24 hours
Percentage of time with SpO2 below target range over period of observation
Time frame: 24 hours
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